GapMind for catabolism of small carbon sources

 

Alignments for a candidate for livJ in Desulfovibrio zosterae DSM 11974

Align Leucine-, isoleucine-, valine-, threonine-, and alanine-binding protein; LIVAT-BP; Leu/Ile/Val/Thr/Ala-binding protein (characterized)
to candidate WP_027720403.1 H589_RS0101635 branched-chain amino acid ABC transporter substrate-binding protein

Query= SwissProt::P21175
         (373 letters)



>NCBI__GCF_000425265.1:WP_027720403.1
          Length = 377

 Score =  212 bits (540), Expect = 1e-59
 Identities = 123/341 (36%), Positives = 194/341 (56%), Gaps = 3/341 (0%)

Query: 14  AMAIAGFASYSMAADTIKIALAGPVTGPVAQYGDMQRAGALMAIEQINKAGGVNGAQ-LE 72
           A AI    S  + A T+K+   GP+TGP A  G+  + G L A+E + + GG+ G   +E
Sbjct: 11  AAAILMLGSGMVFAKTLKLGTMGPLTGPYAADGNDIKNGVLTAVEVVKENGGIPGFDSIE 70

Query: 73  GVIYDDACDPKQAVAVANKVVNDGVKFVVGHVCSSSTQPATDIYEDEGVLMITPSATAPE 132
            +  D AC+P+QAVA ANK++N+G   VVG  CSS+T PA+++ ++E ++MITP++T  +
Sbjct: 71  VLPQDTACEPRQAVATANKLINEGANGVVGAYCSSATLPASEVLDEESIIMITPASTNEK 130

Query: 133 ITSRGYKLIFRTIGLDNMQGPVAGKFIAERYKDKTIAVLHDKQQYGEGIATEVKKTVEDA 192
           +TSRG   +FR  G D+ QG +A KF+ E+   K++ ++ DK  Y +G+A  V+K  + A
Sbjct: 131 VTSRGLPYMFRMCGRDDDQGAIALKFMQEKLGAKSVYIVDDKTAYSQGLADGVEKMAKAA 190

Query: 193 GIKVAVFEGLNAGDKDFNALISKLKKAGVQFVYFGGYHPEMG-LLLRQAKQAGLDARFMG 251
           GIKV   E +N GDKDF+A+++K+K       Y    +   G L+L QAK+ G+ A  + 
Sbjct: 191 GIKVLGHEHVNQGDKDFSAILTKVKTDNPDVFYMSMQNSATGALMLIQAKRMGIKAVRLA 250

Query: 252 PEGVGNSEITAIAGDASEGMLATLPRAFEQDPKNKALIDAFKAKNQDPSGIFVLPAYSAV 311
            + V + ++  IA DA+E +  T     +  P  K     ++ K  +P G +   AY + 
Sbjct: 251 QDAVYHPQLIEIAKDAAEDVYLTFGFIDDNAPAYKEFYAKYQPKYGNP-GAYSGYAYDSA 309

Query: 312 TVIAKGIEKAGEADPEKVAEALRANTFETPTGNLGFDEKGD 352
               K ++ AG  DPEKV   L    ++  T ++ F   GD
Sbjct: 310 IAYLKAVKAAGSTDPEKVKAELMKLDYDGATKHIKFKANGD 350


Lambda     K      H
   0.316    0.133    0.377 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 316
Number of extensions: 18
Number of successful extensions: 4
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 373
Length of database: 377
Length adjustment: 30
Effective length of query: 343
Effective length of database: 347
Effective search space:   119021
Effective search space used:   119021
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.6 bits)
S2: 50 (23.9 bits)

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory